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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Brain (London, England : 1878), 2014-08, Vol.137 (Pt 8), p.2329-2345

2014

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Author Correction: TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

Nature communications, 2021-05, Vol.12 (1), p.3165-3165, Article 3165

2021

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CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability

Brain (London, England : 1878), 2022-10, Vol.145 (10), p.3415-3430

2022

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NDUFS6 related Leigh syndrome: a case report and review of the literature

Journal of human genetics, 2019-07, Vol.64 (7), p.637-645

2019

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TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

Nature communications, 2021-03, Vol.12 (1), Article 1924

2021

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A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare Diseases

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10891

2021

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Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Annals of neurology, 2011-03, Vol.69 (3), p.501-508

2011

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HIV-1 TAR RNA: the target of molecular interactions between the virus and its host

Current HIV research, 2005-01, Vol.3 (1), p.61

2005

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Petite Integration Factor 1 (PIF1) helicase deficiency increases weight gain in Western diet-fed female mice without increased inflammatory markers or decreased glucose clearance

PloS one, 2019-05, Vol.14 (5), p.e0203101-e0203101

2019

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Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases

BMC medical genetics, 2018-04, Vol.19 (1), p.57-57, Article 57

2018

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Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives

Frontiers in molecular biosciences, 2020-11, Vol.7, p.590842-590842

2020

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Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

Mitochondrion, 2016-09, Vol.30, p.126-137

2016

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TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress

Molecular and Cellular Biology, 2009-01, Vol.29 (1), p.254-265

2009

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A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs

Molecular genetics and metabolism reports, 2019-12, Vol.21, p.100543-100543, Article 100543

2019

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Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes

Biological research, 2016-01, Vol.49 (4), p.4-4, Article 4

2016

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Small Interfering RNAs against the TAR RNA Binding Protein, TRBP, a Dicer Cofactor, Inhibit Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression and Viral Production

Journal of Virology, 2007-05, Vol.81 (10), p.5121-5131

2007

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Low TRBP Levels Support an Innate Human Immunodeficiency Virus Type 1 Resistance in Astrocytes by Enhancing the PKR Antiviral Response

Journal of Virology, 2005-10, Vol.79 (20), p.12763-12772

2005

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Astrocyte infection by HIV-1: mechanisms of restricted virus replication, and role in the pathogenesis of HIV-1-associated dementia

Current HIV research, 2003-10, Vol.1 (4), p.463

2003

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Two Dimerization Domains in the Trans-activation Response RNA-binding Protein (TRBP) Individually Reverse the Protein Kinase R Inhibition of HIV-1 Long Terminal Repeat Expression

The Journal of biological chemistry, 2001-09, Vol.276 (36), p.33899-33905

2001

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The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

Brain (London, England : 1878), 2012-01, Vol.135 (1), p.23-34

2012

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ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing data

Bioinformatics (Oxford, England), 2022-10, Vol.38 (20), p.4754-4761

2022

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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Neurobiology of aging, 2014-12, Vol.35 (12), p.2884.e1-2884.e4

2014

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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Author Correction: TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability

NDUFS6 related Leigh syndrome: a case report and review of the literature

TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases

A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare Diseases

Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

HIV-1 TAR RNA: the target of molecular interactions between the virus and its host

Petite Integration Factor 1 (PIF1) helicase deficiency increases weight gain in Western diet-fed female mice without increased inflammatory markers or decreased glucose clearance

Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases

Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives

Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress

A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs

Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes

Small Interfering RNAs against the TAR RNA Binding Protein, TRBP, a Dicer Cofactor, Inhibit Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression and Viral Production

Low TRBP Levels Support an Innate Human Immunodeficiency Virus Type 1 Resistance in Astrocytes by Enhancing the PKR Antiviral Response

Astrocyte infection by HIV-1: mechanisms of restricted virus replication, and role in the pathogenesis of HIV-1-associated dementia

Two Dimerization Domains in the Trans-activation Response RNA-binding Protein (TRBP) Individually Reverse the Protein Kinase R Inhibition of HIV-1 Long Terminal Repeat Expression

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing data

Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

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